{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Electroencephalography+%28EEG%29&page=2", "query": { "intervention": "Electroencephalography (EEG)", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Electroencephalography+%28EEG%29&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-29T20:49:14.371Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT06104280", "title": "Medications for Opioid Use Disorder Photosensitive Retinal Ganglion Cell Function, Sleep, and Circadian Rhythms: Implications for Treatment", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Opioid Use Disorder", "Sleep Disturbance" ], "interventions": [ { "name": "Post-Illumination Pupillary Response (PIPR)", "type": "OTHER" }, { "name": "Polysomnography", "type": "OTHER" }, { "name": "Multiple Sleep Latency Test", "type": "OTHER" }, { "name": "Ecological Momentary Assessments", "type": "BEHAVIORAL" }, { "name": "Actigraphy", "type": "DEVICE" }, { "name": "DLMO", "type": "OTHER" }, { "name": "Melatonin Suppression Test", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL", "DEVICE" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 200, "start_date": "2025-01-06", "completion_date": "2029-01-01", "has_results": false, "last_update_posted_date": "2026-08-11", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT06104280" }, { "nct_id": "NCT03405662", "title": "Impact of Photobiomodulation (PBM) on Biomarkers of Alzheimer's Disease", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alzheimer Disease" ], "interventions": [ { "name": "Vielight Neuro Gamma", "type": "DEVICE" }, { "name": "Sham Vielight Neuro Gamma", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 23, "start_date": "2018-08-16", "completion_date": "2021-01-01", "has_results": true, "last_update_posted_date": "2022-07-01", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 2, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03405662" }, { "nct_id": "NCT05128344", "title": "A Study to Evaluate Safety and Efficacy of AMZ002 Treatment, Compared With Vigabatrin in Participants With Infantile Spasms", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Spasms, Infantile" ], "interventions": [ { "name": "AMZ002 injectable solution, 0.5mg/mL", "type": "DRUG" }, { "name": "Vigabatrin, oral", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Amzell", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "2 Months", "maximum_age": "24 Months", "sex": "ALL", "summary": "2 Months to 24 Months" }, "enrollment_count": 0, "start_date": "2023-04", "completion_date": "2025-12", "has_results": false, "last_update_posted_date": "2023-04-20", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 12, "location_summary": "Aurora, Colorado • Miami, Florida • Orlando, Florida + 8 more", "locations": [ { "city": "Aurora", "state": "Colorado" }, { "city": "Miami", "state": "Florida" }, { "city": "Orlando", "state": "Florida" }, { "city": "Orlando", "state": "Florida" }, { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05128344" }, { "nct_id": "NCT06644573", "title": "Evaluating the Efficacy and Safety of PROSOMNIA Sleep Therapy™ in Patients With Sleep Deprivation and Chronic Insomnia", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Chronic Insomnia", "Sleep Deprivation", "REM Behavior Disorder", "REM Sleep Behavior Disorder", "REM Sleep Measurement", "Insomnia", "Insomnia Related to Specified Disorder", "Insomnia Due to Other Mental Disorder", "Insomnia Comorbid to Psychiatric Disorder", "Insomnia Due to Anxiety and Fear", "Insomnia Related to Another Mental Condition", "Insomnia Disorders", "Idiopathic Hypersomnia", "Sleep Disorders, Circadian Rhythm", "Post Trauma Nightmares", "PTSD - Post Traumatic Stress Disorder", "Sleep Quality", "Anesthesia", "Anxiety", "Depression", "Mental Health", "Alzheimer Disease or Associated Disorder", "Parkinsons", "Circadian Rhythm", "Circadian Dysregulation", "PTSD", "Post-Traumatic", "Post-Traumatic Stress Disorder Complex", "Military Combat Stress Reaction", "Sleep", "Military Activity", "Veterans", "Shift Work Sleep Disorder", "Menopause Related Conditions", "Pain", "Cancer Pain", "Athletes" ], "interventions": [ { "name": "PROSOMNIA Sleep Therapy™ (PSTx)", "type": "PROCEDURE" }, { "name": "Anesthesia-Induced Sleep Therapy", "type": "PROCEDURE" }, { "name": "Diprivan (propofol), Astra-Zeneca", "type": "DRUG" }, { "name": "Continuous EEG Monitoring", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "DRUG", "DEVICE" ], "sponsor": "Nyree Penn", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 100, "start_date": "2025-11-01", "completion_date": "2026-05-01", "has_results": false, "last_update_posted_date": "2025-05-28", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 1, "location_summary": "Aventura, Florida", "locations": [ { "city": "Aventura", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06644573" }, { "nct_id": "NCT07812753", "title": "Modulating Neural Mechanisms of Reward Processing in Tobacco Users", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tobacco Use Disorder" ], "interventions": [ { "name": "PRIME TMS", "type": "DEVICE" }, { "name": "Standard TMS", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Rutgers, The State University of New Jersey", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 54, "start_date": "2026-07-24", "completion_date": "2029-07-15", "has_results": false, "last_update_posted_date": "2026-09-10", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 1, "location_summary": "Newark, New Jersey", "locations": [ { "city": "Newark", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT07812753" }, { "nct_id": "NCT06138808", "title": "5-SENSE Score Validation Study", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Epilepsy Intractable" ], "interventions": [ { "name": "Stereoelectroencephalography (SEEG)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "15 Years", "maximum_age": null, "sex": "ALL", "summary": "15 Years and older" }, "enrollment_count": 400, "start_date": "2024-01-09", "completion_date": "2027-06", "has_results": false, "last_update_posted_date": "2026-06-05", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 4, "location_summary": "Gainesville, Florida • Chicago, Illinois • Durham, North Carolina + 1 more", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Durham", "state": "North Carolina" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06138808" }, { "nct_id": "NCT02658708", "title": "Bright Light on Fatigue in Women Being Treated for Breast Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Breast Neoplasms", "Breast Cancer", "Cancer of Breast", "Cancer of the Breast" ], "interventions": [ { "name": "Bright blue-green light using light visor cap", "type": "OTHER" }, { "name": "Dim red light using light visor cap", "type": "OTHER" }, { "name": "European Organization for Research and Treatment of Cancer-Quality of Life Questionnaire", "type": "OTHER" }, { "name": "Epworth Sleepiness Scale", "type": "OTHER" }, { "name": "Pittsburgh Sleep Quality Index", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Sleep Disturbance", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Cancer-Fatigue", "type": "OTHER" }, { "name": "Digital foot candle datalogging light meter (Extech Instrument, Model SDL400)", "type": "DIAGNOSTIC_TEST" }, { "name": "Polysomnography (Easy Ambulatory 2 Cadwell, Kennewick, WA)", "type": "DIAGNOSTIC_TEST" }, { "name": "Horne-Ostberg Morningness-Eveningness Questionnaire", "type": "OTHER" }, { "name": "Daily Fatigue and Sleep Log", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 19, "start_date": "2015-10-12", "completion_date": "2017-05-09", "has_results": false, "last_update_posted_date": "2017-09-25", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02658708" }, { "nct_id": "NCT05015478", "title": "Rhythmic Light Therapy for Alzheimer's Disease Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mild Cognitive Impairment" ], "interventions": [ { "name": "Tailored Rhythmic Lighting Intervention", "type": "DEVICE" }, { "name": "Placebo Rhythmic Lighting Intervention", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Icahn School of Medicine at Mount Sinai", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "55 Years", "maximum_age": null, "sex": "ALL", "summary": "55 Years and older" }, "enrollment_count": 52, "start_date": "2022-01-10", "completion_date": "2023-09-12", "has_results": true, "last_update_posted_date": "2026-06-23", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 2, "location_summary": "Menands, New York • New York, New York", "locations": [ { "city": "Menands", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05015478" }, { "nct_id": "NCT03322371", "title": "Validation of Frontal EEG to Formal Polysomnography in the ICU", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep Deprivation", "Sleep" ], "interventions": [ { "name": "2-lead limited electroencephalography recording", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 44, "start_date": "2017-11-06", "completion_date": "2020-01-01", "has_results": false, "last_update_posted_date": "2021-06-08", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT03322371" }, { "nct_id": "NCT00137384", "title": "Movement-Related Brain Networks Involved in Hand Dystonia", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Movement Disorder", "Focal Dystonia" ], "interventions": [], "intervention_types": [], "sponsor": "National Institute of Neurological Disorders and Stroke (NINDS)", "sponsor_class": "NIH", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2005-08-25", "completion_date": "2018-04-27", "has_results": false, "last_update_posted_date": "2018-05-01", "last_synced_at": "2026-09-29T20:49:14.371Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT00137384" } ] }